Down-regulation of sirtuin 3 is associated with poor prognosis in hepatocellular carcinoma after resection

被引:49
|
作者
Wang, Jia-Xing [1 ]
Yi, Yong [1 ]
Li, Yi-Wei [1 ]
Cai, Xiao-Yan [1 ]
He, Hong-Wei [1 ]
Ni, Xiao-Chun [1 ]
Zhou, Jian [1 ]
Cheng, Yun-Feng [2 ]
Jin, Jian-Jun [2 ]
Fan, Jia [1 ]
Qiu, Shuang-Jian [1 ,2 ]
机构
[1] Fudan Univ, Chinese Minist Educ, Key Lab Carcinogenesis & Canc Invas, Liver Canc Inst,Zhongshan Hosp, Shanghai 200433, Peoples R China
[2] Fudan Univ, Zhongshan Hosp, Biomed Res Ctr, Shanghai 200433, Peoples R China
来源
BMC CANCER | 2014年 / 14卷
基金
中国国家自然科学基金;
关键词
Sirtuin; Hepatocellular carcinoma; Prognosis; HISTONE DEACETYLASE INHIBITOR; GASTRIC-CANCER CELL; TRICHOSTATIN-A; OXIDATIVE STRESS; IN-VITRO; APOPTOSIS; GROWTH; EXPRESSION; METABOLISM; ACTIVATION;
D O I
10.1186/1471-2407-14-297
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Sirtuin 3 (Sirt3), one of the seven Sirtuins family members, plays critical roles in the progression of multiple cancer types. However, its role in the prognosis of hepatocellular carcinoma (HCC) has not yet been investigated systematically. Methods: The correlation of Sirtuins expression with prognosis of HCC was determined by immunohistochemistry (IHC) in a large HCC patient cohort (n = 342). Expression of Sirt3 in tumoral and peritumoral tissues of HCC patients were further determined by western blotting (WB). Results: IHC and WB studies both showed a decreased expression of Sirt3 in tumoral tissues compared with peritumoral tissues (P = 0.003 for IHC, P = 0.0042 for WB). Decreased expression of Sirt3 in both tumoral and peritumoral tissues was associated with increased recurrence probability and decreased overall survival rate by univariate analyses (intratumoral Sirt3: P = 0.011 for TTR, P = 0.001 for OS; peritumoral Sirt3: P = 0.017 for TTR, P = 0.023 for OS), the prognostic value was strengthened by multivariate analyses (intratumoral Sirt3: P = 0.031 for TTR, P = 0.001 for OS; peritumoral Sirt3: P = 0.047 for TTR, P = 0.031 for OS). Intratumoral Sirt3 also showed a favorable prognostic value in patients with BCLC stage A (TTR, P = 0.011; OS, P < 0.001). In addition, we found that IHC studies of other sirtuin members showed a decreased expression of Sirt2, Sirt4 and Sirt5 and an increased expression of Sirt1, Sirt6 and Sirt7 in intratumoral tissues compared with peritumoral tissues. In contrast to Sirt3, other members did not showed a remarkable correlation with HCC prognosis. Conclusions: Down-regulation of intratumoral and peritumoral Sirt3 were both associated with poor outcome in HCC, moreover, intratumoral Sirt3 was a favorable prognostic predictor in early stage patients.
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页数:9
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